HGVS | Genome Assembly |
---|---|
NC_000007.14:g.147877725del , CM000669.2:g.147877725del | GRCh38 |
NC_000007.13:g.147574817del , CM000669.1:g.147574817del | GRCh37 |
NC_000007.12:g.147205750del | NCBI36 |
NG_007092.2:g.1766365del | |
NG_007092.3:g.1766725del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361727.8:c.2099-25840del MANE Select | ENSP00000354778.3:n.2099-25840del | |
ENST00000636870.1:n.1961-25840del | ||
ENST00000637825.1:n.1582-25840del | ||
ENST00000361727.7:c.2099-25840del | ENSP00000354778.3:n.2099-25840del | |
ENST00000455301.2:n.34-25840del | ||
ENST00000627772.2:n.272-25840del | ||
NM_014141.5:c.2099-25840del | NP_054860.1:n.2099-25840del | |
XM_006715919.1:c.587-25840del | XP_006715982.1:n.587-25840del | |
NM_014141.6:c.2099-25840del MANE Select | NP_054860.1:n.2099-25840del |